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CompletedNCT02089074Updated Mar 30, 2017

Systematic Follow up of Drug Treatment by Pharmacists in Secondary Prevention After Transient Ischemic Attack

An interventional study of Drug use counselling in Ischemic Attack, Transient and Stroke, sponsored by Norwegian University of Science and Technology. Completed at 6 sites in Norway. Open to participants aged 18 Years to 90 Years. Per ClinicalTrials.gov, last updated 2017-03-30.

Sponsored by Norwegian University of Science and Technology · Not applicable, Interventional, and Treatment

From the registry’s dates

  • Registered 1 year 4 months after the study started (first participant enrolled Nov 2012, registered Mar 2014).
Phase
Not applicable
Study type
Interventional
Enrollment
265
Allocation
Randomized
Ages
18 Years to 90 Years
Sex
All
01

Study summary

Use of drugs is an important factor in secondary prophylaxis after transient ischemic attack (TIA), but studies show that adherence to the prescribed drugs is often poor. This randomised controlled trial aims to investigate whether a systematic follow up of drug treatment using medication reconciliation, medication reviews and patient counselling by clinical pharmacists, improves adherence and/or decreases cardiovascular events the first three months and the first year after TIA. Patient satisfaction will also be compared between the two groups.

02

Conditions studied

  • Ischemic Attack, Transient
  • Stroke

Keywords

  • Secondary Prevention
  • Pharmacists
  • Directive Counseling
  • Medication Adherence
  • Patient Compliance
03

In context

Ischemic Attack, Transient

293 studies on the registry are indexed under Ischemic Attack, Transient; 64 are open to participants now.

This study's enrollment of 265 is above the median of 206 across 164 interventional studies indexed under Ischemic Attack, Transient.

Browse Ischemic Attack, Transient studies →

Lead sponsor

Norwegian University of Science and Technology is the lead sponsor of 487 studies on the registry; 52 are open to participants now.

Counted across the registry records on this site, refreshed daily.

04

Who can participate

Ages eligible
18 Years to 90 Years
Sexes eligible
All
Accepts healthy volunteers
No

Eligibility criteria

Inclusion Criteria:

  • Probable or possible transient ischemic attack
  • Residing in Central Norway
  • Examined within 2 weeks after the onset of symptoms
  • Modified Rankin Scale 3 or less and living at home
  • enrolled in the MIDNOR-TIA study NCT02038725
  • Informed consent
05

Study design

Phase
Not applicable
Primary purpose
Treatment
Allocation
Randomized
Intervention model
Parallel assignment
Masking
None (open label)
Enrollment
265 participants (actual)

Study arms

  • Experimental
    drug use counselling

    Pharmacist conducting drug reconciliation, medication reviews and drug use counselling during hospitalisation. Follow up telephone calls 1 week, 1 month, 2 months and three months after discharge from hospital

    Behavioral: Drug use counselling

  • No intervention
    Control group

    The patients in the control group receive no intervention just treatment and follow up according to national standards

Interventions

  • BehavioralDrug use counselling
06

What researchers measure

Primary outcomes

  1. adherence to drug treatment in secondary prevention after TIA

    self reporting of adherence

    Time frame: 3 months

Secondary outcomes

  1. adherence to drug treatment in secondary prevention after TIA

    self reporting of adherence

    Time frame: 1 year

  2. Persistence

    Persistence measured by control of filled prescriptions

    Time frame: 3 months

  3. Incidence of stroke and cardiovascular events and deaths

    Measured by using data from national health registries

    Time frame: 3 months

  4. degree of disability or dependence in the daily activities

    measured by modified Rankin Scale and indirectly by level of care

    Time frame: 3 months

  5. patient satisfaction

    Measured by using data from the Norwegian Stroke Registry

    Time frame: 3 months

  6. Persistence

    Persistence measured by control of filled prescriptions

    Time frame: 1 year

  7. Incidence of stroke and cardiovascular events and deaths

    Measured by using data from national health registries

    Time frame: 1 year

  8. degree of disability or dependence in the daily activities

    measured by modified Rankin Scale and indirectly by level of care

    Time frame: 1 year

  9. patient satisfaction

    Measured by using data from the Norwegian Stroke Registry

    Time frame: 1 year

07

Study locations

6 sites
  • Kristiansund Sykehus
    Kristiansund, Norway
  • Levanger Sykehus
    Levanger, Norway
  • Molde Sykehus
    Molde, Norway
  • Namsos Sykehus
    Namsos, Norway
  • St Olavs Hospital
    Trondheim, Norway
  • Ålesund Sykehus
    Ålesund, Norway
08

Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on Mar 30, 2017, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
09

Registry details

Key details

Study ID
NCT02089074
Lead sponsor
Norwegian University of Science and Technology
Collaborators
St. Olavs Hospital, Helse Midt-Norge, Sykehusapotekene i Midt Norge
Responsible party
Sponsor
First posted
Mar 17, 2014
Start date
Nov 2012
Primary completion
Sep 2015
Completion
Jun 2016
Last update
Mar 30, 2017

Study contacts

Bent Indredavik, PhD, Prof
study director · Norwegian University of Science and Technology

Oversight

Data monitoring committee
No
FDA-regulated drug
No
FDA-regulated device
No
View the source record on ClinicalTrials.gov ↗

Not currently enrolling

This study is completed, as verified in Mar 2017. You cannot join it, but the record below documents what was studied.

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